Rezai-Delui H, Mamoori G, Sadri-Mahvelati E, Noori N M
Department of Radiology, Mashad University, Ghaen Hospital, Iran.
Skeletal Radiol. 1994 Aug;23(6):411-9. doi: 10.1007/BF00204601.
Nine cases of progressive pseudorheumatoid chondrodysplasia in subjects aged 7-60 years are reported. Six of them were members of one large family with several consanguineous marriages. Evaluation of six generations of this family suggested an autosomal recessive mode of inheritance. The presentation of the disease was between the ages of 3 and 8 years with waddling gait and fusiform swelling of the interphalangeal joints of the hands, clinically resembling juvenile rheumatoid arthritis. Most of the other joints become progressively involved, with crippling disability. One of the patients had typical features of Blount disease at presentation.
报告了9例年龄在7至60岁的进行性假类风湿性软骨发育不良病例。其中6例来自一个有多次近亲结婚的大家庭。对这个家族六代人的评估表明其遗传方式为常染色体隐性遗传。该病通常在3至8岁发病,表现为蹒跚步态和手部指间关节梭形肿胀,临床上类似于幼年类风湿性关节炎。大多数其他关节也会逐渐受累,导致严重残疾。其中一名患者在初诊时具有典型的布朗特病特征。